Genetics University — Research, Education, Medical Genetics
Knowledge Hub

Gene entry

GLI3

GLI family zinc finger 3

Chromosome
7
Cytoband
7p14.1
Variants (rsID)
84

GLI3 is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 7 (region 7p14.1). Its official name is “GLI family zinc finger 3”. The reference table lists 84 variants (rsID) for this gene.

ShareE-MailWhatsAppLinkedInXFacebookTelegram

Clinically classified variants

19 reference-table entries with clinical significance.

  • rs113629469Benignsingle nucleotide variantGreig cephalopolysyndactyly syndrome|Polydactyly|Pallister-Hall syndrome
  • rs114615136Benignsingle nucleotide variantGreig cephalopolysyndactyly syndrome|Polydactyly|Pallister-Hall syndrome
  • rs145419251Benignsingle nucleotide variantPallister-Hall syndrome|Greig cephalopolysyndactyly syndrome|Polydactyly|Pallister-Hall syndrome|Greig cephalopolysyndactyly syndrome
  • rs201070431Benignsingle nucleotide variantGreig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Polydactyly
  • rs35280470Benignsingle nucleotide variantPallister-Hall syndrome|Greig cephalopolysyndactyly syndrome|Polydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs35364414Benignsingle nucleotide variantPolydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs62622373Benignsingle nucleotide variantGreig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Greig cephalopolysyndactyly syndrome|Polydactyly|Pallister-Hall syndrome
  • rs77126593Benignsingle nucleotide variantGreig cephalopolysyndactyly syndrome|Polydactyly|Pallister-Hall syndrome
  • rs79049330Benignsingle nucleotide variantPolydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs79703713Benignsingle nucleotide variantPolydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs121917710Conflicting interpretationssingle nucleotide variantPostaxial polydactyly, type A1/B|Pallister-Hall syndrome|Greig cephalopolysyndactyly syndrome|Polydactyly|Polydactyly, postaxial, type A1|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs148043302Conflicting interpretationssingle nucleotide variantPallister-Hall syndrome|Polydactyly|Greig cephalopolysyndactyly syndrome|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs148226583Conflicting interpretationssingle nucleotide variantGreig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Polydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs149248727Conflicting interpretationssingle nucleotide variantGreig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Polydactyly
  • rs199875457Conflicting interpretationssingle nucleotide variantGreig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Polydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs186337909Likely benignsingle nucleotide variant
  • rs200913720Likely benignsingle nucleotide variantPolydactyly|Greig cephalopolysyndactyly syndrome|Pallister-Hall syndrome
  • rs121917716Uncertain significancesingle nucleotide variantGreig cephalopolysyndactyly syndrome|Hirschsprung disease, susceptibility to, 1|Pallister-Hall syndrome|Greig cephalopolysyndactyly syndrome
  • rs140772904Uncertain significancesingle nucleotide variantGreig cephalopolysyndactyly syndrome|Pallister-Hall syndrome|Greig cephalopolysyndactyly syndrome

Other listed variants

Public references

Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.